NDC 0220-9066 Chestal Kids Pellets

Antimony Potassium Tartrate,Bryonia Alba Root,Protortonia Cacti, Drosera Rotundifolia - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0220-9066
Proprietary Name:
Chestal Kids Pellets
Non-Proprietary Name: [1]
Antimony Potassium Tartrate, Bryonia Alba Root, Protortonia Cacti, Drosera Rotundifolia Whole, Ipecac, Pulsatilla Vulgaris Whole, Rumex Crispus Root, Spongia Officinalis Skeleton, Roasted, Lobaria Pulmonaria
Substance Name: [2]
Antimony Potassium Tartrate; Bryonia Alba Root; Drosera Rotundifolia; Ipecac; Lobaria Pulmonaria; Protortonia Cacti; Pulsatilla Vulgaris; Rumex Crispus Root; Spongia Officinalis Skeleton, Roasted
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Boiron
    Labeler Code:
    0220
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-27-2020
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    4 MM

    Product Packages

    NDC Code 0220-9066-41

    Package Description: 80 PELLET in 1 TUBE

    NDC Code 0220-9066-42

    Package Description: 2 TUBE in 1 BOX / 80 PELLET in 1 TUBE

    Product Details

    What is NDC 0220-9066?

    The NDC code 0220-9066 is assigned by the FDA to the product Chestal Kids Pellets which is a human over the counter drug product labeled by Boiron. The generic name of Chestal Kids Pellets is antimony potassium tartrate, bryonia alba root, protortonia cacti, drosera rotundifolia whole, ipecac, pulsatilla vulgaris whole, rumex crispus root, spongia officinalis skeleton, roasted, lobaria pulmonaria. The product's dosage form is pellet and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 0220-9066-41 80 pellet in 1 tube , 0220-9066-42 2 tube in 1 box / 80 pellet in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Chestal Kids Pellets?

    Antimonium tartaricum 6C HPUS ... Helps loosen thick mucusBryonia 3C HPUS ... Relieves dry and painful coughCoccus cacti 3C HPUS ... Relieves cough associated with a tickling in the throatDrosera 3C HPUS ... Relieves barking cough worse at nightIpecacuanha 3C HPUS ... Relieves cough associated with nauseaPulsatilla 6C HPUS ... Relieves wet cough during the day becoming dry at nightRumex crispus 6 HPUS ... Relieves dry cough triggered by cold airSpongia tosta 3C HPUS ... Relieves dry, croupy, and barking coughSticta pulmonaria 3C HPUS ... Relieves nighttime hacking coughTemporarily relieves dry cough due to minor throat and bronchial irritation as may occur with a cold, helps relieve chest congestion due to common colds by loosening mucus and thinning bronchial secretions to make coughs more productive

    What are Chestal Kids Pellets Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Chestal Kids Pellets UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Chestal Kids Pellets Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".